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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
Term:Intellectual Developmental Disorder, Autosomal Dominant, FRA12A Type
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Accession:DOID:9005790 term browser browse the term
Synonyms:exact_synonym: INTELLECTUAL DISABILITY, FRA12A TYPE;   mental retardation, FRA12A type
 primary_id: MESH:C566980
 alt_id: OMIM:136630


show annotations for term's descendants           Sort by:
Intellectual Developmental Disorder, Autosomal Dominant, FRA12A Type term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Dip2b disco-interacting protein 2 homolog B ISO CTD Direct Evidence: marker/mechanism
ClinVar Annotator: match by term: Intellectual disability, FRA12A type		 OMIM
CTD
ClinVar		 PMID:17236128 PMID:25741868 NCBI chr 7:131,174,575...131,350,417
Ensembl chr 7:131,174,567...131,349,092 		JBrowse link
G Tecpr2 tectonin beta-propeller repeat containing 2 ISO ClinVar Annotator: match by term: Intellectual disability, FRA12A type ClinVar PMID:25741868 PMID:28492532 NCBI chr 6:129,899,541...130,001,975
Ensembl chr 6:129,899,636...130,001,974 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18969
    Developmental Disease 14401
      Neurodevelopmental Disorders 6848
        intellectual disability 4300
          Intellectual Developmental Disorder, Autosomal Dominant, FRA12A Type 2
Path 2
Term Annotations click to browse term
  disease 18969
    disease of anatomical entity 18249
      nervous system disease 14091
        central nervous system disease 12432
          brain disease 11669
            disease of mental health 8321
              developmental disorder of mental health 5554
                specific developmental disorder 4518
                  intellectual disability 4300
                    Intellectual Developmental Disorder, Autosomal Dominant, FRA12A Type 2
paths to the root